Right Ventricular Strain in Detecting Subclinical Right Ventricular Systolic Dysfunction in Psoriatic Arthritis Patients: Relation to Serum Endostatin Level
1 other identifier
observational
60
1 country
1
Brief Summary
The aim is to assess early right ventricular systolic dysfunction in psoriatic arthritis patients using RV strain echocardiography
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jul 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 19, 2025
CompletedFirst Posted
Study publicly available on registry
July 1, 2025
CompletedStudy Start
First participant enrolled
July 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2027
July 1, 2025
May 1, 2025
1.8 years
May 19, 2025
June 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Detecting subclinical right ventricular systolic dysfunction in PsA patients
Detecting subclinical right ventricular systolic dysfunction in PsA using 2D strain transthoracic echo and its relation to serum endostatin level
Up to 24 months
Study Arms (2)
Control
30 control group matched as regards BMI, age and sex will be subjected to transthoracic echo and measuring serum endostatin level.
Cases of Psoriatic arthritis patients
30 PsA patients will be subjected to transthoracic echo, measuring serum endostatin level and modified composite psoriatic disease activity index
Eligibility Criteria
30 patients with PsA and 30 matched healthy controls
You may qualify if:
- Psoriatic arthritis patients according to CASPAR criteria
- Psoriatic arthritis patients without overt cardiovascular symptoms
- Patients with age between 20 to 50 years of age
You may not qualify if:
- Other systemic autoimmune diseases
- Patients with a history of known valvular disease, atrial fibrillation or any other arrhythmia , heart failure, ischemic cardiomyopathy severe obstructive pulmonary diseases and metabolic syndrome.
- Patients with medical disorders as renal, congenital heart diseases, hematological disorders and cancer patients.
- Patients taking certain drugs that have been confirmed to be risk factors for PAH such as appetite suppressant intake drugs (aminorex, fenfluramine derivatives and benfluorex) and chemotherapeutic agents.
- Family history of myocardial infarction, cerebrovascular disease or sudden death before the age of 65y in females and 55 y in males.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ain Shams University
Cairo, Abbassia, 00202, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 19, 2025
First Posted
July 1, 2025
Study Start
July 1, 2025
Primary Completion (Estimated)
April 1, 2027
Study Completion (Estimated)
April 1, 2027
Last Updated
July 1, 2025
Record last verified: 2025-05